mLabs® Cardiac Panel 3 (UDI 06974703166353)
Manufactured by Micropoint Biotechnologies Co., Ltd.
Device Regulatory Overview
The mLabs® Cardiac Panel 3 (Model/Catalog Number: M101-091011) is a medical device manufactured by Micropoint Biotechnologies Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160706 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- M101-091011
- Product Code / EMDN
- W0102160706
- Device Name
- mLabs® Cardiac Panel 3
- Database Sync Date
- 2026-08-09 16:51:46
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of mLabs® Cardiac Panel 3?
The registered manufacturer of record for mLabs® Cardiac Panel 3 is Micropoint Biotechnologies Co., Ltd..
What is the Primary UDI-DI identifier for mLabs® Cardiac Panel 3?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974703166353.
What classification code is assigned to this device?
This device is registered under product classification code W0102160706.
Similar Classification Devices (W0102160706)
Other Devices by Micropoint Biotechnologies Co., Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint